Total oxidant and antioxidant status and paraoxonase 1 levels ofchildren with noncystic fibrosis bronchiectasis

por GEDİK, Ahmet Hakan, ÇAKIR, Erkan, VEHAPOĞLU TÜRKMEN, Aysel, ÖZER, Ömer Faruk, KAYGUSUZ, Sare Betül
Publicado 2020

FOXA2 as a Candidate Gene Responsible for Congenital Panhypopituitarism: A Review of the Literature

por Correia, Jorge César, Corral, Laura Gómez, Kaygusuz, Sare Betül, Gualtieri, Angelica, Gaston-Massuet, Carles
Publicado 2021

MON-LB061 Cushing Syndrome Due to an Adrenocortical Carcinoma in a Baby with Atypical Beckwith-Wiedemann Syndrome

por Bereket, Abdullah, Eltan, Mehmet, Cerit, Kivilcim, Kaygusuz, Sare Betül, Ates, Esra, Ergelen, Rabia, Eker, Nursah, Bagci, Pelin, Turan, Serap, Guran, Tulay
Publicado 2019

Efficacy of the Novel Degludec/Aspart Insulin Co-formulation in Children and Adolescents with Type 1 Diabetes: A Real-life Experience with One Year of IDegAsp Therapy in Poorly Con...

por Kırkgöz, Tarık, Eltan, Mehmet, Kaygusuz, Sare Betül, Yavaş Abalı, Zehra, Helvacıoğlu, Didem, Seven Menevşe, Tuba, Gürpınar Tosun, Büşra, Güran, Tülay, Bereket, Abdullah, Turan, Serap
Publicado 2022

A Rare Cause of Hypophosphatemia: Raine Syndrome Changing Clinical Features with Age

por Eltan, Mehmet, Alavanda, Ceren, Yavas Abali, Zehra, Ergenekon, Pinar, Yalındag Ozturk, Nilufer, Sakar, Mustafa, Dagcinar, Adnan, Kirkgoz, Tarik, Kaygusuz, Sare Betul, Gokdemir, Yasemin, Elcioglu, Huriye Nursel, Guran, Tulay, Bereket, Abdullah, Ata, Pinar, Turan, Serap
Publicado 2020

Broad-spectrum XX and XY gonadal dysgenesis in patients with a homozygous L193S variant in PPP2R3C

por Cicek, Dilek, Warr, Nick, Yesil, Gozde, Kocak Eker, Hatice, Bas, Firdevs, Poyrazoglu, Sukran, Darendeliler, Feyza, Direk, Gul, Hatipoglu, Nihal, Eltan, Mehmet, Yavas Abali, Zehra, Gurpinar Tosun, Busra, Kaygusuz, Sare Betul, Seven Menevse, Tuba, Helvacioglu, Didem, Turan, Serap, Bereket, Abdullah, Reeves, Richard, Simon, Michelle, Mackenzie, Matthew, Teboul, Lydia, Greenfield, Andy, Guran, Tulay
Publicado 2021